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dc.contributor.authorBautista, Mayka
dc.contributor.authorMartínez de Ilarduya Sáez de Asteasu, Domingo Antxon
dc.contributor.authorAlla Bedahnane, Abdelilah
dc.contributor.authorMuñoz Guerra, Sebastián
dc.contributor.otherUniversitat Politècnica de Catalunya. Departament d'Enginyeria Química
dc.date.accessioned2016-09-27T10:06:31Z
dc.date.available2017-09-01T00:30:30Z
dc.date.issued2016-09-01
dc.identifier.citationBautista, M., Martinez de Ilarduya, A., Alla, A., Muñoz, S. Poly(butylene succinate) ionomers and their use as compatibilizers in nanocomposites. "Polymer composites", 1 Setembre 2016, vol. 37, núm. 9, p. 2603-2610.
dc.identifier.issn0272-8397
dc.identifier.urihttp://hdl.handle.net/2117/90227
dc.description.abstractA series of low-molecular-weight poly(butylene succinate-co-glutarate-co-2-trimethylammonium chloride glutarate) terpolyester ionomers containing 35% mol of total glutarate units but varying in the content of charged units were synthesized by polycondensation at mild temperatures using a scandium catalyst. The terpolyester ionomers started to decompose at the temperatures of >175°C and all of them were semicrystalline and have glass transition temperature similar to poly(butylene succinate) (PBS). These terpolyesters were used to compatibilize the nanocomposites made of PBS-cloisite (CL) prepared by melt extrusion. X-ray diffraction revealed that an intercalated structure was present in these nanocomposites. The thermal properties of the three-component mixtures did not differ substantially from those of PBS–CL but the mechanical properties were significantly improved by the addition of the ionomer, in particular tenacity. The beneficial effect afforded by the terpolyester ionomer was attributed to its ability for strengthening the binding between the PBS and the nanoclay.A series of low-molecular-weight poly(butylene succinate-co-glutarate-co-2-trimethylammonium chloride glutarate) terpolyester ionomers containing 35% mol of total glutarate units but varying in the content of charged units were synthesized by polycondensation at mild temperatures using a scandium catalyst. The terpolyester ionomers started to decompose at the temperatures of >175°C and all of them were semicrystalline and have glass transition temperature similar to poly(butylene succinate) (PBS). These terpolyesters were used to compatibilize the nanocomposites made of PBS-cloisite (CL) prepared by melt extrusion. X-ray diffraction revealed that an intercalated structure was present in these nanocomposites. The thermal properties of the three-component mixtures did not differ substantially from those of PBS–CL but the mechanical properties were significantly improved by the addition of the ionomer, in particular tenacity. The beneficial effect afforded by the terpolyester ionomer was attributed to its ability for strengthening the binding between the PBS and the nanoclay.
dc.format.extent8 p.
dc.language.isoeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectÀrees temàtiques de la UPC::Enginyeria química
dc.subject.lcshPolymers
dc.subject.lcshPolyurethanes
dc.subject.otherPBS
dc.subject.otherPoly(butylene succinate)
dc.subject.otherionomers
dc.subject.othernanocomposites
dc.subject.othermechanical properties
dc.titlePoly(butylene succinate) ionomers and their use as compatibilizers in nanocomposites
dc.typeArticle
dc.subject.lemacPolímers
dc.subject.lemacPoliuretans
dc.contributor.groupUniversitat Politècnica de Catalunya. POL - Polímers Industrials Avançats i Biopolímers Tecnològics
dc.identifier.doi10.1002/pc.23454
dc.description.peerreviewedPeer Reviewed
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/doi/10.1002/pc.23454/full
dc.rights.accessOpen Access
local.identifier.drac18817794
dc.description.versionPostprint (author's final draft)
dc.relation.projectidinfo:eu-repo/grantAgreement/MINECO/1PE/MAT2012-38044-C03-03
local.citation.authorBautista, M.; Martinez de Ilarduya, A.; Alla, A.; Muñoz, S.
local.citation.publicationNamePolymer composites
local.citation.volume37
local.citation.number9
local.citation.startingPage2603
local.citation.endingPage2610


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